Canonical Allele Identifier: CA1752467006
Gene: NOS3 HGNC NCBI

Linked Data

dbSNP Id: rs1802273623

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150992474G>C , CM000669.2:g.150992474G>C GRCh38
NC_000007.13:g.150689562G>C , CM000669.1:g.150689562G>C GRCh37
NC_000007.12:g.150320495G>C NCBI36
NG_011992.1:g.6416G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297494.8:c.-52+1174G>C MANE Select ENSP00000297494.3:n.-52+1174G>C
ENST00000297494.7:c.-52+1174G>C ENSP00000297494.3:n.-52+1174G>C
ENST00000461406.5:c.-149+1174G>C ENSP00000417143.1:n.-149+1174G>C
NM_000603.4:c.-52+1174G>C NP_000594.2:n.-52+1174G>C
NM_000603.5:c.-52+1174G>C MANE Select NP_000594.2:n.-52+1174G>C